A role for coding functional variants in HNF4A in type 2 diabetes susceptibility
Aims/hypothesis: Rare mutations in the gene HNF4A, encoding the transcription factor hepatocyte nuclear factor 4α (HNF-4A), account for ∼5% of cases of MODY and more frequent variants in this gene may be involved in multifactorial forms of diabetes. Two low-frequency, non-synonymous variants in HNF4...
Prif Awduron: | , , , , , , , , , , , , , , , , , , , , , , |
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Fformat: | Journal article |
Iaith: | English |
Cyhoeddwyd: |
2011
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